OUR

Achievements

Our dedicated team at MedOut is assigned to each project, ensuring a daily activity, close follow-up, and effective implementation of the agreed strategy.

We also provide daily reports from the assigned team and bi-monthly reports to clients for progress and updates.

Additionally, our team checks and reviews all certificates and technical data, prepares and submits files, and performs technical and auditing functions.

Our business approach at MedOut is focused on implementing effective strategies to achieve our desired goals.

We pass through preparatory meetings to agree on the most effective approach to accomplish our clients' objectives.

We also seek to innovate more services and expand into new regions while maintaining and enhancing our current success.

At MedOut, we continuously monitor local and regional developments to target new business opportunities and challenges to expand our business activities further.

We understand the pressures healthcare and government institutions face in today's rapidly changing medical device industry, and we are committed to serving our clients with high quality and efficiency throughout the preparation, submission, and close follow-up of our projects.

At MedOut, we take pride in our achievements, leveraging our experience and awareness of regulations and requirements for medical device registration in Egypt.

We have successfully found solutions to problems in certificates and product technicalities and helped prepare FSCs, different types of agreements, and relations to fulfill the MOH requirements and finalize the registration process.

Our regulatory consulting services have helped many manufacturers worldwide, including the top ten medical device companies such as Philips, Stryker, Abbott Vascular (in addition to registration in the MOH and marketing consultation in Egypt), and Terumo (in addition to registration in the MOH and marketing consultation in Egypt).

We have also assisted many other companies in obtaining licenses from CAPA, including registration, variation, scientific committee approval, and importation approvals.